Department of Life Science, National Institute of Technology, Rourkela, India.
Eur J Cancer Prev. 2020 Nov;29(6):556-564. doi: 10.1097/CEJ.0000000000000587.
Cancer is an unpleasant, painful disease. It is one of the most devastating diseases worldwide diminishing many lives. Many genetic and epigenetic changes occur before cancer develops. Mutation in SETD2 gene is one such example. RNA splicing, DNA damage repair, DNA methylation and histone methylation are some of the biological processes mediated by SETD2. SETD2 (histone H3 lysine 36 methyltransferase) is a frequently mutated gene in different types of cancer. Loss of SETD2 is associated with worse prognosis and aggressive phenotypes. Histone modification is one of the epigenetic regulation having a significant effect on gene regulation. N6-methyladenosine (m6A) mRNA modification is a well-known posttranscriptional modification playing a pivotal role in many normal and pathological processes affecting RNA metabolism. SETD2 catalyses H3K36 trimethylation and in turn H3K36me3 guides the deposition of m6A on nascent RNA transcripts. Finally, this review summarizes the deep understanding of the role of SETD2 in RNA methylation/modification and how SETD2 mutation contributes to tumour development.
癌症是一种令人不快和痛苦的疾病。它是全球最具破坏性的疾病之一,使许多人的生命受到威胁。在癌症发展之前,会发生许多遗传和表观遗传变化。SETD2 基因的突变就是一个例子。RNA 剪接、DNA 损伤修复、DNA 甲基化和组蛋白甲基化是 SETD2 介导的一些生物学过程。SETD2(组蛋白 H3 赖氨酸 36 甲基转移酶)是不同类型癌症中经常发生突变的基因。SETD2 的缺失与预后不良和侵袭性表型相关。组蛋白修饰是一种对基因调控有显著影响的表观遗传调控方式。N6-甲基腺苷(m6A)mRNA 修饰是一种众所周知的转录后修饰,在影响 RNA 代谢的许多正常和病理过程中起着关键作用。SETD2 催化 H3K36 三甲基化,反过来 H3K36me3 指导 m6A 在新生 RNA 转录本上的沉积。最后,本文综述了对 SETD2 在 RNA 甲基化/修饰中的作用以及 SETD2 突变如何促进肿瘤发生的深入理解。